FdaApplication
ANDA 072164
Identifiers
- fda_app_no: ANDA072164
Properties
| Property | Value |
|---|---|
| applicant_name | WATSON LABORATORIES INC |
| application_type | ANDA |
| approval_date | 1988-06-01 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MAPROTILINE HYDROCHLORIDE | MAPROTILINE HYDROCHLORIDE | 75MG | TABLET;ORAL |
1 product